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- Synthesis and photocatalytic H2 evolution properties of four titanium-oxo-clusters based on a cyclohex-3-ene-1-carboxylate ligand. Mei-Yan Gao, Shumei Chen, Lan-Xia Hu, Lei Zhang, Jian Zhang
, Dalton Trans.
, 2017
, 46
, 10630
- Application of chemical P-450 model systems to studies on drug metabolism. Part X. Novel hydroxylactonization of γ,δ- and β,γ- unsaturated carboxylic acids with an iron porphyrin–iodosylbenzene system. Masakatsu Komuro, Tsunehiko Higuchi, Masaaki Hirobe
, J. Chem. Soc., Perkin Trans. 1
, 1996
, 2309
- Amphiphilic allylation of arylidene-1,3-oxazol-5(4H)-one using bis-π-allylpalladium complexes: an approach to synthesis of cyclohexyl and cyclohexenyl α-amino acids. Afaf R. Genady, Hiroyuki Nakamura
, Org. Biomol. Chem.
, 2011
, 9
, 7180
- Mutational biosynthesis of a FK506 analogue containing a non-natural starter unit. Yeon Hee Ban, Jong Hyun Lee, Gyo Rim Gu, Boram Lee, SangJoon Mo, Ho Jeong Kwon, Yeo Joon Yoon
, Mol. BioSyst.
, 2013
, 9
, 944
- Dimethyl sulfoxide–trimethylsilyl bromide–amine system as a bromonium ion source containing a potential internal nucleophile; unusual bromolactonisation of cyclohex-3-enecarboxylic acid derivatives. Kazuyuki Miyashita, Akira Tanaka, Hiroaki Mizuno, Masahiro Tanaka, Chuzo Iwata
, J. Chem. Soc., Perkin Trans. 1
, 1994
, 847
- Reaction of 1 : 2 : 3 : 6-tetrahydrobenzaldehyde with alkali. E. G. E. Hawkins, D. J. G. Long, F. W. Major
, J. Chem. Soc.
, 1955
, 1462
- Dehydro-aromatization of cyclohexene-carboxylic acids by sulfuric acid: critical route for bio-based terephthalic acid synthesis. Fei Wang, Zhaohui Tong
, RSC Adv.
, 2014
, 4
, 6314
- Cinchona alkaloid derivative modified Fe3O4 nanoparticles for enantioselective ring opening of meso-cyclic anhydrides. Sanjiv O. Tomer, Hemant P. Soni
, New J. Chem.
, 2022
, 46
, 2495
- Enhancing menaquinone-7 production in recombinant Bacillus amyloliquefaciens by metabolic pathway engineering. Jian-Zhong Xu, Wei-Liu Yan, Wei-Guo Zhang
, RSC Adv.
, 2017
, 7
, 28527
- Can electrostatic catalysis of Diels–Alder reactions be harnessed with pH-switchable charged functional groups?. Heather M. Aitken, Michelle L. Coote
, Phys. Chem. Chem. Phys.
, 2018
, 20
, 10671